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WHSC1 is involved in DNA damage, cellular senescence and immune response in hepatocellular carcinoma progression

Wolf–Hirschhorn syndrome candidate 1 (WHSC1) is a transcriptional regulatory protein that encodes a histone methyltransferase to control H3K36me2 modification. WHSC1 was upregulated and associated with poor prognosis in HCC. The elevated WHSC1 likely due to the alterations of DNA methylation or RNA...

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Bibliographic Details
Published in:Journal of cellular and molecular medicine 2023-05, Vol.27 (10), p.1436-1441
Main Authors: Yan, Jia, Zhang, Ming Yang, Lin, Jing, Li, Ke Xin, Zhao, Zhi Min, Gao, Yu Min, Deng, Xiu Ling, Wang, Chang Shan, Wang, Hai Sheng
Format: Article
Language:English
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Summary:Wolf–Hirschhorn syndrome candidate 1 (WHSC1) is a transcriptional regulatory protein that encodes a histone methyltransferase to control H3K36me2 modification. WHSC1 was upregulated and associated with poor prognosis in HCC. The elevated WHSC1 likely due to the alterations of DNA methylation or RNA modification. WHSC1 perhaps form a chromatin cross talk with H3K27me3 and DNA methylation to regulate transcription factors expression in HCC. Functional analysis indicated that WHSC1 was involved in DNA damage repair, cell cycle, cellular senescence and immune regulations. Furthermore, WHSC1 was associated with the infiltrating levels of B cell, CD4+, Tregs and macrophage cells. Therefore, our findings suggested that WHSC1 might function as a promotor regulator to affect the development and progression of HCC. Thus, WHSC1 could be a potential biomarker in predicting the prognosis and therapeutic target for patients with HCC.
ISSN:1582-1838
1582-4934
DOI:10.1111/jcmm.17743